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Method Article

Whole Cell Electrophysiology of Primary Cultured Murine Enterochromaffin Cells

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DOI:

10.3791/58112

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September 26th, 2018

 ,  ,  ,  ,  , 

* These authors contributed equally

In This Article

Summary

Enterochromaffin (EC) cells comprise a small subset of gastrointestinal epithelial cells. EC cells are electrically excitable and release serotonin, yet difficulties in culturing and identifying EC cells have limited physiological studies. The method presented here establishes a primary culture model amenable to examination of single EC cells by electrophysiology.

Abstract

Enterochromaffin (EC) cells in the gastrointestinal (GI) epithelium constitute the largest subpopulation of enteroendocrine cells. As specialized sensory cells, EC cells sense luminal stimuli and convert them into serotonin (5-hyroxytryptamine, 5-HT) release events. However, the electrophysiology of these cells is poorly understood because they are difficult to culture and to identify. The method presented in this paper outlines primary EC cell cultures optimized for single cell electrophysiology. This protocol utilizes a transgenic cyan fluorescent protein (CFP) reporter to identify mouse EC cells in mixed primary cultures, advancing the approach to obtaining high-quality recordings of whole cell electrophysiology in voltage- and current-clamp modes.

Introduction

The gastrointestinal (GI) epithelium is a diverse community consisting of several cell types. Enteroendocrine cells comprise roughly 1% of all epithelial cells, and enterochromaffin (EC) cells are the largest enteroendocrine cell population1. Recent studies show that enteroendocrine2 and EC3,4 cells are electrically excitable. We are interested in understanding primary EC cell electrophysiology. Thus, the purpose of this study was to establish primary EC cell cultures optimized for whole cell electrophysiology.

Existing EC cell lines t....

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Protocol

All methods described here have been approved by the Institutional Animal Care and Use Committee (IACUC) of Mayo Clinic. The primary cell culture portion of this protocol is based on previously published methods that can be referenced for further details10. All experimental procedures must be approved by the (IACUC), and all experiments must be performed in accordance with relevant guidelines and regulations.

1. Culture Preparation

  1. Media.
    1. Prepare EC cell complete culture media with high glucose [4500mg/L] Dulbecco's Modified Eagle Medium (DMEM) supplemented with 5% Fetal B....

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Results

Cultures:
Primary murine epithelial cells made from a transgenic Tph1-CFP model attach to dishes after 4 hours and are ready for physiological experiments between 24 to 72 h. When culture conditions had not been optimized, the epithelial cell culture consisted of large clumps, floating cellular debris, damaged membranes, and weak CFP signal in the EC cells (Figure 1A). Cultures that have been optimized for electrophysiolo.......

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Discussion

Fully understanding EC cell function requires a high-quality primary culture method to generate cells for whole cell electrophysiology. Primary cultures of GI epithelium had traditionally been difficult due to low survival. Alleviating this confounding factor, the present method yields cultures of singular EC cells from either small or large bowel that are capable of surviving for several days.

We found that the following were critical for improving the quality of cultures to be suitable for e.......

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Acknowledgements

The authors thank Mrs. Lyndsay Busby for administrative assistance and Mr. Robert Highet from Mayo Clinic Division of Engineering for design and 3D printing of the culture dish insert. This work was supported by NIH K08 to AB (DK106456), Pilot and Feasibility Grant to AB from Mayo Clinic Center for Cell Signaling in Gastroenterology (NIH P30DK084567) and 2015 American Gastroenterological Association Research Scholar Award (AGA RSA) to AB and NIH R01 to GF (DK52766).

....

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
100 mm x 15 mm culture dishCorning (Falcon)351029
Transfer PipetteFisherbrand13-711-7M
10 mL serological pipetteCorning (Falcon) 357551
50 mL ConicalCorning (Falcon) 352098
15 mL ConicalCorning (Falcon) 352097
1,000 mL Barrier Pipet TipsThermo Scientific (Art)2079EKeep sterile
MatTek Glass Bottom DishesMatTek CorporationP35G-1.5-14-CKeep sterile
Micro-dissection Forceps - Very Fine, Extra-Long PointsFine Science ToolsSB12630M
Surgical Scissors-SharpNasco14002-14
Micro-Dissection ScissorsNascoSB46568M
Monoject Hypo Needle, 21 G x 1" A, 100/BXCovidien8881250172
 Tg(Tph1-CFP)1Able/J MiceJacksonStock # 028366Use male or female mice between the ages of 4-7 weeks
Microfil nonmetallic syringe needles (34 gauge, 67 mm)World Precision InstrumentsMF34G-5
Parafilm "M" Laboratory FilmPechiney Plastic Packaging
R6101Dow Corning
6 mL syringe with regular luer tipMonoject
3 mL syringe with regular luer tipMonoject
Electrophysiology Equipment
AmplifierMolecular DevicesAxopatch 200B
Data acquisition system (daq)Molecular DevicesDigidata 1440A
Signal conditionerMolecular DevicesCyberAmp 320
SoftwareMolecular DevicespClamp 10.6

References

  1. Rindi, G., Leiter, A. B., Kopin, A. S., Bordi, C., Solcia, E. The "normal" endocrine cell of the gut: changing concepts and new evidences. Annals of the New York Academy of Sciences. 1014, 1-12 (2004).
  2. Rogers, G. J., et al.

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